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1190875-39-8

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1190875-39-8 Usage

Uses

Different sources of media describe the Uses of 1190875-39-8 differently. You can refer to the following data:
1. 1-(1-(tert-Butoxycarbonyl)piperidin-4-yl)-1H-pyrazol-4-ylboronic acid is used in the preparation of triazolopyrazine derivatives for treating hyperproliferative disorders.
2. 1-(Boc-piperidin-4-yl)-pyrazole-4-boronate is used in the preparation of triazolopyrazine derivatives for treating hyperproliferative disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 1190875-39-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,0,8,7 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1190875-39:
(9*1)+(8*1)+(7*9)+(6*0)+(5*8)+(4*7)+(3*5)+(2*3)+(1*9)=178
178 % 10 = 8
So 1190875-39-8 is a valid CAS Registry Number.

1190875-39-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(1-BOC-Piperidino)pyrazole-4-boronic acid

1.2 Other means of identification

Product number -
Other names [1-[1-[(2-methylpropan-2-yl)oxycarbonyl]piperidin-4-yl]pyrazol-4-yl]boronic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1190875-39-8 SDS

1190875-39-8Relevant articles and documents

Preparation method of crizotinib

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Paragraph 0040-0043, (2017/01/23)

The invention discloses a preparation method of crizotinib. An intermediate (V) is prepared through boric acid condensation, so that the defects of instable borate serving as a raw material, complexity in operation, low yield and large-scale production difficulty in the prior art are overcome. The preparation method is low in cost, simple and convenient to operate, high in yield, good in optical purity and suitable for large-scale production.

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